Canonical Allele Identifier:
CA1215982352
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192800631T= , CM000663.2:g.192800631T= | GRCh38 |
| NC_000001.10:g.192769761T= , CM000663.1:g.192769761T= | GRCh37 |
| NC_000001.9:g.191036384T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429211.2:n.61T= |